کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2550435 1560571 2016 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Melatonin protects female rats against steatosis and liver oxidative stress induced by oestrogen deficiency
ترجمه فارسی عنوان
ملاتونین موش های ماده را در برابر استئاتوز و استرس اکسیداتیو کبدی ناشی از کمبود استروژن محافظت می کند
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی کاردیولوژی و پزشکی قلب و عروق
چکیده انگلیسی

AimsMelatonin has been shown to protect cells against oxidative and inflammatory damage via endocrine, paracrine and autocrine actions. Postmenopausal condition is associated with a high incidence of many features of metabolic syndrome including obesity, steatosis and liver oxidative injuries. The aim of this work was to investigate whether treatment with melatonin improves metabolic disturbances associated with oestrogen deficiency in ovariectomised (OVX) rats.Main methodsOVX and control (CON) female rats were treated with melatonin (10 mg/kg × day for 3 weeks, p.o.). Body weight gain, adiposity index, plasma biochemical parameters, liver lipid content, hepatic mitochondrial respiration, fatty acid oxidation and mitochondrial H2O2 generation and the activity of the most important enzymatic and non-enzymatic reactive oxygen species (ROS) scavenger systems were measured.Key findingsIn OVX rats, melatonin suppressed lipid accumulation and cellular oxidative stress in the liver. There was a reduction in the levels of carbonylated proteins in the mitochondria and cytosol, reduction in the malondialdehyde contents in the liver homogenates, stimulation of cytosolic glutathione peroxidase and glutathione reductase activities and restoration of reduced glutathione contents to normal levels.SignificanceExogenous melatonin protects the liver of OVX rats against steatosis and cellular oxidative stress, possibly via activation of antioxidant enzymes related to glutathione metabolism and by a direct radical scavenging activity.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Life Sciences - Volume 157, 15 July 2016, Pages 178–186
نویسندگان
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